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Associate Director, Pharmacovigilance Scientist, Oncology

Job LocationCambridge
EducationNot Mentioned
Salary400.00 - 550.00 per day
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract , full-time

Job Description

*Associate Director, Pharmacovigilance Scientist, Oncology - Global Pharma - 12-month contract - Cambridge* My client is a Global Biopharmaceutical company, and they have a position available for an Associate Director, Pharmacovigilance Scientist for an initial 12- month contract, INSCOPE.Hybrid working, 2 days in office.As an Associate Director, PS Scientist, you will be involved in aggregating, reviewing, analysing and interpreting safety-related data to generate information to support safety decision-making by prescribers, patients and payers, with the ultimate goal of protectingpatients. You will apply your PV, oncology and scientific experience, knowledge, and skills to deliver all aspects of safety documentation, including authoring and / or providing strategic safety input to regulatory documents, e.g., regulatory reports, healthauthority responses and the safety content of marketing authorisation applications. Main Responsibilities:

  • Supporting study start-ups and protocol reviews
  • Supporting teams implementing safety strategy into protocols
  • Bringing theory from health authorities regarding protocols
  • Assisting study designs.
In order to apply for the Associate Director, Pharmacovigilance Scientist contract, you should possess extensive experience in the field of pharmacovigilance within the pharmaceutical industry, including experience at data analysis / evaluation and scientificwriting (beyond standard texts in periodic reports). You should possess a strong background in clinical trial drug safety and have experience with protocols, IB, ICFs etc and working with Health Authorities. Experience in Oncology products and antibody drugconjugates & immune checkpoint inhibitors would be a major plus.Before you apply for this position it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK. To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on .

Keyskills :
Drug SafetyOncologyPharmacovigilanceProtocolsAssociate DirectorIB'sClinical Trials PVICF's

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